A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232450



Internal ID20799490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66226901..66391300hg38UCSC Ensembl
chr9:42129880..42294312hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38164400
hg19164433
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441901
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232450
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00386


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